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saasCNV  

Somatic Copy Number Alteration Analysis Using Sequencing and SNP Array Data
View on CRAN: Click here


Download and install saasCNV package within the R console
Install from CRAN:
install.packages("saasCNV")

Install from Github:
library("remotes")
install_github("cran/saasCNV")

Install by package version:
library("remotes")
install_version("saasCNV", "0.3.4")



Attach the package and use:
library("saasCNV")
Maintained by
Zhongyang Zhang
[Scholar Profile | Author Map]
First Published: 2016-05-18
Latest Update: 2016-05-18
Description:
Perform joint segmentation on two signal dimensions derived from total read depth (intensity) and allele specific read depth (intensity) for whole genome sequencing (WGS), whole exome sequencing (WES) and SNP array data.
How to cite:
Zhongyang Zhang (2016). saasCNV: Somatic Copy Number Alteration Analysis Using Sequencing and SNP Array Data. R package version 0.3.4, https://cran.r-project.org/web/packages/saasCNV. Accessed 01 May. 2025.
Previous versions and publish date:
No previous versions
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Complete documentation for saasCNV
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